Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_assertion> ?p ?o ?g. }
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- NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_assertion type Assertion NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_head.
- NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_assertion description "[Analysis of GNAS1 and overlapping transcripts identifies the parental origin of mutations in patients with sporadic Albright hereditary osteodystrophy and reveals a model system in which to observe the effects of splicing mutations on translated and untranslated messenger RNA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_provenance.
- NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_assertion evidence source_evidence_curated NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_provenance.
- NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_assertion SIO_000772 12624854 NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_provenance.
- NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_assertion wasDerivedFrom uniprot-2016 NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_provenance.
- NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_assertion wasGeneratedBy ECO_0000218 NP2555.RA7AdjOmDNEGgmEnjdovOexdIShbRvshTlFWlwFnit50I130_provenance.